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The theory and practice of industrial pharmacy / Leon Lachman, Herbert A. Lieberman, and Joseph L. Kanig.

By: Contributor(s): Material type: TextTextPublication details: Philadelphia, Pennsylvania : Lea & Febiger, c1976Edition: Second EditionDescription: xii, 767 pages : illustrations ; 25 cmISBN:
  • 081210532X
Subject(s): LOC classification:
  • RS 192 .L33 1976
Contents:
1. Preformulation -- 2. Kinetic principles and stability testing -- 3. Biopharmaceutics -- 4. Theories of dispersion -- 5. Pharmaceutical suspensions -- 6. Emulsions -- 7. Semisolids -- 8. Suppositories -- 9. Pharmaceutical aerosols -- 10. Compaction and compression -- 11. Tablets -- 12. Tablet coating -- 13. Capsules -- 14. Sustained action dosage -- 15. Milling -- 16. Mixing -- 17. Drying -- 18. Clarification and filtration -- 19. Liquids -- 20. Sterilization -- 21. Sterile products -- 22. Pilot plant scale-up -- 23. Production management -- 24. Packaging materials science -- 25. Quality control: process -- 26. Drug regulatory affairs.
Summary: The second edition required considerable updating of existing chapters, elimination of certain chapters from the first edition, and inclusion of new chapters on preformulation, production management, packaging materials, science, and drug regulatory affairs.
Item type: Books
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Holdings
Item type Current library Home library Collection Call number Copy number Status Date due Barcode
Books Books National University - Manila LRC - Annex Relegation Room Pharmacy GC RS 192 .L33 1976 (Browse shelf(Opens below)) c.1 Available NULIB000003984

Includes bibliographical references and index.

1. Preformulation -- 2. Kinetic principles and stability testing -- 3. Biopharmaceutics -- 4. Theories of dispersion -- 5. Pharmaceutical suspensions -- 6. Emulsions -- 7. Semisolids -- 8. Suppositories -- 9. Pharmaceutical aerosols -- 10. Compaction and compression -- 11. Tablets -- 12. Tablet coating -- 13. Capsules -- 14. Sustained action dosage -- 15. Milling -- 16. Mixing -- 17. Drying -- 18. Clarification and filtration -- 19. Liquids -- 20. Sterilization -- 21. Sterile products -- 22. Pilot plant scale-up -- 23. Production management -- 24. Packaging materials science -- 25. Quality control: process -- 26. Drug regulatory affairs.

The second edition required considerable updating of existing chapters, elimination of certain chapters from the first edition, and inclusion of new chapters on preformulation, production management, packaging materials, science, and drug regulatory affairs.

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